ArticlePDF Available

Distribution of fatty acids and total lipids in five tissues of edible snail helix lucorum (l., 1758) from the southeast of turkey

Authors:

Abstract

This investigation was carried out on fatty acid compositions and total lipid quantities in selected tissues (gonad, mantle, digestive gland, cephalopedal and whole body) o f Helix lucorum with the aim o f evaluating biochemical and nutritional value o f edible snail parts. C16:0, C18:0, C18:1ra9, C18:2ra6, C20:2ra6 and C20:4ra6 were found as dominant components. C18:2ra6 (24.44%) and C20:4ra6 (17.49%) were present in fair amounts in the digestive gland and gonad, respectively. The gonad and mantle had a good proportion o f C20:2ra6 and the cephalopedal contained significant amount o f C20:1ra9. XPUFA levels were higher than XSFA and XMUFA levels in all tissues. Overall ratio o f Xra6/Xra3 was defined as follow: gonad, 9.07; mantle, 7.26; cephalopedal, 6.02; whole body, 4.86; digestive gland, 4.06. Among the organs, digestive gland and gonad showed the highest p roportion of total lipid. Consequently, the study revealed that tissues o f the snail are a good source for PUFA (polyunsaturated fatty acids), essential fatty acids C18:2ra6, C20:4o>6 (precursors of eicosanoids) and other omega 6 family fatty acids, however the total lipid contents were not found at the expected amount. In numerous studies, it is stated that snail meat has several advantages including rich minerals, essential amino and fatty acids and high content o f PUFA. Their meat is believed to be a factor affecting higher life span and lower cancer rate in some countries. High amount o f C18:2ra6, C20:4ra6 and PUFA make them important nutrition due to preventing cardiovascular disease, inflammatory disorders and retina and brain development.
PAPER
DISTRIBUTION OF FATTY ACIDS AND TOTAL LIPIDS
IN FIVE TISSUES
OF EDIBLE SNAIL HELIX LUCÜRUM (L., 1758)
FROM THE SOUTHEAST OF TURKEY
I. EN
Sirnak University, Engineering Faculty,
Department of Energy Systems Engineering, Sirnak, Turkey
Corresponding author: ekinihsan@gmail.com
AB ST R ACT
Th is investigation was carried out on fa tty acid c o m positions a n d total lipid quan tities in select
ed tissu e s (gonad, m antle, diges tive glan d, cepha lopeda l and whole body) o f Helix lucorum with the
aim o f evaluating bio c h em ica l and nutritional va lu e o f edible snail parts. C16:0, C18:0, C18:1ra9,
C18:2ra6, C20:2ra6 and C20:4ra6 w ere found as dom inant comp on e n ts. C18:2ra6 (24.44%) and
C20:4ra6 (17.49% ) were present in fair am ounts in the digestive gla n d and gonad, res p ectively. Th e
gonad and m an tle had a g o o d propo rtio n o f C20:2ra6 and the ceph alo pedal contain ed sign ifican t
amou n t o f C20:1ra9. X PUFA levels w ere hig h er th an XSFA and XM UFA le v els in all tissues. Overall
ratio o f Xra6/Xra3 was defined as follow: gonad, 9.07; m an tle, 7.26; cephalopedal, 6.02; w hole body,
4.86; d igestive gland, 4.06. Am on g th e organs, digestive gland and gona d show ed the highest pro
portion o f total lipid. Consequently, the stud y revea led that tis su es o f the snail are a good so u rce
for P UF A (polyu n saturated fatty acids), essential fatty acids C18:2ra6, C20:4o>6 (pre cu rsors o f ei-
cosanoids) and other om eg a 6 fam ily fatty acids, h ow ever the to tal lipid c o ntents w e r e not foun d
at th e expected am o unt. In num ero u s stu d ies, it is sta ted tha t snail m eat has several a dvan tag
es inc lud ing rich m inerals, essen tial a m ino and fatty acid s an d high c o ntent o f PUFA. Th e ir m ea t
is b e lieved to be a fa ctor a ffectin g h igh e r life sp a n and low er c a ncer rate in som e countries . High
amou n t o f C18:2ra6, C20:4ra6 and P UF A m ake th em im portant n u trition due to preventing ca r d i
ovascula r disease, infla m mato ry disorders a n d retin a and brain development.
- Keywords: fatty acids, edible land snail, Helix lucorum, tissues, total lipid -
56 Ital. J. Food Sci., vol. 26 - 2014
IN T RO DU CT IO N
Hu m an bein g s have be en con sum ed sn ails
fo r th ous a nds of years and recen tly snails have
been used as fo od fo r m illio n s o f people w orld
w id e , pa rticu larly in so me E urop ea n co un
tries (JESS a n d MARKS, 1995; MURPHY, 2001).
France im ports edible sn a ils to a certain extent
to m eet th e n eeds of its m a rk e t. T ur k ey is one
of th e im po rtant coun tries w hich e xport snails
to F ranc e (ÖZOG u l et al., 2005) an d o th er E u
ropea n countries; Greece, Germ any, Italy and
Sp ain (YILDIRIM and KEBAPÇI, 2 0 04 ). S om e
com mercially im p ortant edible sn a ils in c lu ding
Cryptomphalus aspersus (Helix aspersa), The-
ba pisana, Eobania verm iculata, Cantareus ap-
ertus, Helix asemnis, Helix cincta and H elix lu-
corum (YILDIRIM and KEBAPÇI, 2004) are living
in Tu rkish territories.
Now ad ays, fa tty acids ga in more and more
im po r ta n ce be c au se o f th e nu trition al an d
hea lth a spects. E sp e cia lly , th e c on su m ption
of m arine produ cts rich in om ega 3 fatty ac
id s such as C20:5ra3 and C22:6ra3 ha s in
creas ed due to re sea rch es de mon stra t in g the
ben e fic ia l effect of these fatty acids in p re ven t
in g dis ease s inc lu din g ca r d iova scu lar disease,
in fla mm ato ry disorde rs , re tin a and b ra in d e
velop me nt (MILETIC et al., 1991; Ö Z OG ul et
al., 2005 ; MILINSK et al., 20 0 6). Sna il m ea t is
fo un d to be a facto r a ffe ctin g h igh e r life span
and low er ca nc er rate in Cre ta n Pe o ple co m
pare d with th ose o f con tine n tal E ur o pe (YILDI
RIM and KEBAPÇI, 200 4 ).
In ad d ition to ba s ic in form a tion ab out th e cul
tivation and h arvestin g of edible snails is n e ces
sary, the ir nutritional com position also shou ld
be well illum inated. Th e protein con ten t of ed
ible sn ail is well docum en ted (ÇAGILTAY et al.,
2011); h ow ever there is only lim ited inform a
tion on th eir tissues lip ids and fatty acids c o m
position. Th e purpose o f the presen t stu d y was
to p rovide quan titativ e and qualitative inform a
tion about the lipid and fatty acid com p osition
of som e im portant tissues of H. lucorum from the
Southeast o f Turkey.
MA T ER IA L S A N D M ETH OD S
Sam plin g
Helix lucorum snails were co llected in Ap ril
20 1 2 from the region o f Hevsel G ardens loca ted
in Diy arbakır (Altitude: 583 m, C oordinate: N 37°
55.2 / E 40° 13.8’), Turkey. Individu ally, twelve
sn ails (three for tissues, th ree for w h ole body,
six for tota l lipid) sim ilar size (len gth: 5 ± 0.50
cm, w et flesh weig h t: 14 ± 0.80 g) were sam pled
fo r each tissue lipid analysis. Th e s n ails shells
were rem oved and divided into five groups and
th eir org a ns (gonad , m antle , digestive gland,
cep h alo p ed al and w ho le body) w ere disse ct
ed out. Then, tissues of each experim ental set
were co ndition e d in polye th ylene b a gs and kept
at -80°C un til chem ical a nalysis.
Ch em ical analysis
Dissec ted tissu es su ch as gonad, man tle, di
gestive g lan d , c ep h alo pe d al a n d wh ole bo dy
were an alyzed in triplicate for proximate com
position: lip id con tent of the sn ails by the BLIGH
and DYER (1959) meth od. Autoxidatio n of u n
sa tu rated fatty acids w a s m inim ized b y adding
50 ^L of 2% butyla ted hydroxytoluen e in chloro
fo r m to each sam ple during the extraction p ro
cess. N2 wa s u sed fo r dryin g process o f lipid ex
tracts. To tal lipids w e re p ut into reaction vials
and the fatty acids w ere transm ethylate d by re-
fluxing the fra c tions in acid ified (sulfu ric acid)
m e th ano l for 90 minu te at 85°C. FAM Es (fatty
acid m ethyl esters) of the tissu es w ere extract
ed fro m the reactio n vials three tim es with hex
ane and concen trated (STANLEY-SAMUELSON and
DADD, 1983). The total lip id quantitie s o f the tis
su es were p e r form ed acco rdin g to the method o f
FOLCH et al. (1957).
FAM Es we r e a n alyzed by ca pilla r y gas ch ro
m a tograp h y (GC) using H ew lett Packard (W ilm
ington, D E ) g a s chrom atograp h (m odel 6890), a
DB -23 ca p illary c o lum n (60 m x 0.2 5 mm i.d.
x 0.250 ^m film thickn ess and B o nd e d 50%
cyano p ropyl) (J. & W. Sc ientific, Fo lsom , CA),
a fla me ionization detector, and H ew lett- P ac k
ard C he m Statio n software. The in jectio n port
and the de tec to r tem pe ratures w ere 270° and
28 0 °C, resp e c tively . Th e split ratio w as 1:20.
Th e flow rates o f com pressed air an d h ydroge n
we r e 300 m L/ m in and 30 m L/ m in, res pe c tiv e
ly. Ca r r ier ga s w as he lium (2.8 mL/m in). The
ov en tem perature w as prog r a mm ed at a ra te o f
6.5 °C/ m in from 130°C (1 min hold ) to 170°C,
th en inc r e a sed a t a ra te of 2.7 5 °C/ min to a
21 5 °C, then a g a in inc re a sed a t a rate o f 40°C /
m in to 230°C, w a s he ld for 12 min . Each tis
su e fatty acid s perce n tages and s p ectra o f FA
M E s a re ob tained by HP 3 3 65 C hem Station
com pu ter program . FAM Es ex istence and re
te ntion tim es we re determ ined b y co mparing
th e sp e c tra o f a uthen tic sta nd a rds (Sigm a-Al-
drich C hem ica ls). Indiv idual F AM E w as iden ti
fied b y com pa ris o ns w ith the chrom atog ra p hic
beh aviors o f a u thentic sta n dards.
Statistica l an a lyses
The re s ults w ere expressed as m ean valu es ±
S.D. (S tan d a rd Devia tion ). A ll a n alytica l de te r
m ina tions were p erform ed in triplicate and the
m e a n values w e re rep orted. The analyses w ere
perform ed using a com merc ial sta tistical pro
gram (SPSS 20). Th e pe rcen tages of fa tty acid
were co m pared by An ov a variance analy s is with
5% significan ce level. Tu key s test was u sed for
co operation o f average values.
Ital. J. Food Sci., vol. 26 - 2014 57
RES ULT S AN D D ISCU S SION
Nutrient conten t of edible an d nonedible sn ails
wa s studied up to s o m e extent. Comp a red with
in form ation on fa tty acid com position, lipid data
corre lated w ith ph ysio logical and enviro n men
tal factors in the snails is n o tably lim ited in the
literature. Som e o f the c o mm erc ia lly im po r
ta n t ed ible and w ild snails in clu ding H. aspersa
(ÇAGILTAY et al., 2011), H. aspersa maxima (MI-
LINSK et al., 2006), H. pomatia (ÖZOGul et al.,
2005), E. vermiculata (STAVRAKAKIS et al., 1989),
Helix sp., Ha.plotrema sportella., Vespericola co
lumbiana (ZHU et al., 1994) an d land slu gs Arion
ater, Limax maximus, Prophysaon andersoni (ZHU
et al., 1994) have been stu died in term s o f fatty
acid contents. A lm ost all d a ta inclu ded in mol-
lu s c a n lipid study conce rn the en tire organism
and only few reports on the tissu e fatty a cids are
ava ilab le (RAKSHIT et al., 1997). Telescopium tel
eskoptum (RAKSHIT et al., 1997), Bellam ya ben-
galensis, Pila globosa (MISRA et al., 2002), Unio
elongatulus (EKİN and BASHAN, 2010), Macoma
balthica (WENNE and POLAK, 1989), Argopecten
purpuratus (CAERS et al., 1999) are some o f the
tissue studied m ollusc species. Alth oug h H. lu-
corum , H. cincta, H. asemnis, T. pisana, E. ver-
miculata, C. asperses and C. apertus are m ost
ly distributin g edible sn ails o f T urk ey (YILDIRIM
and KEBAPÇI, 2004), there is no t enough stu dy
on th e ir to tal lipid a nd fatty acid composition.
C 16 : 0 (6 .7 -1 0.1 % ), C 18 :0 (9 .1 -1 0.7 % ),
C18:1o>9 (12.1-1 5 .7% ), C18:2ra6 (11.6-15.2% ),
C20:4ra6 (13 .5-14.3% ) w ere the m ajo r fatty ac
ids in P. andersoni, A. ater, L. maxim us slugs and
C16:0 (7.1-9.6%), C18:0 (8.9-1 0 .6% ), C18:1ra9
(10.0-12.2%), C18:2o>6 (11.0 -15.7%), C20:2ra6
(9.1 -12.1 %), C20:4ra6 (13 .8-16.9% ) w e r e major
fatty acid in Helix sp. H. sportella., V columbiana
sn ails (ZH U et al., 1994). Th e high percen tages of
th ese fa tty acids also foun d in so m e other fresh
wa ter snails Theodoxus jordani, Pyrigula barroi-
si, Melanopsis praemorsum, Melanoides tubercu-
lata, (GO et al., 2002), M. praem orsa (EKİN et al.,
2011), in edible land snails H. aspersa (ÇAGILTAY
et al., 2011), H. pom atia (ÖZOGul et al., 2004)
and in non e d ible snail T. telescopium (RAKSHIT
et al., 1997). In com pariso n with above studies,
the m ajor fatty acid profiles of H. lucorum shown
sim ila rities. C16:0 (8.95-1 4 .04% ), C18:0 (8.39
11.65% ), C18:1ra9 (11 .2 3-1 8 .20 %), C18:2ra6
(1 6 .21-24 .44% ), C20:2ra6 (4 .78-10 .5 2 %) an d
C20:4ra6 (8.8 9 -17.49%) we r e fou nd to be pre
dominant com ponent in all tissu es (Table 1). The
hig h est va lue of C20:4ra6 (17.49 % ) and C18:2ra6
(24.44%) we r e detected in the go nad a nd di
gestive glan d, respectively (Table 2). C18:1ra9
acid w as foun d in h igh am ount in wh ole body
(18.2 0 % ) a n d in the dig e s tive gland (17.18% )
(T a ble 2). H ow ever C20:2ra6 w as dete c ted in
high percentage in the gona d (10.52% ) and in
the mantle (10.09% ) (Table 2). Th e mostly im
porta n t essential fa tty acid, C18:2ra6 wa s fo u nd
in high co n ce ntra tio n in th e d igestive gla n d
(24.4 4% ) (Tab le 2). An im als (except som e in v er
tebrates) c a nno t synthesize C18:2ra6 fro m oth er
co m pon e n ts, they are obliged to take it fro m di
ets a n d m ust con su me for prope r health. A diet
only deficient in C18:2ra6 ca u ses most ab no r
m a lities such as poor gro w th, skin lesions, h a ir
loss, po or wou n d healing, fatty liver a n d rep ro
ductive failure. In T. telescopium snail, C16:0 was
12.9% in th e digestive gland, 26.2% in th e m an
tle, 21.1% in the ce p halo p edal and C16:1ra7 wa s
11.3% in th e dig e stive gland, 6.1% in the m an
tle, 4.9% in the cephalop edal. M oreover, there
were also som e stran ge resu lts in T. telescopium
snail, for in stan ce C18:3ra3 w as not detected in
the d igestive gland an d m an tle, but it w a s found
10.7% in the cephalopedal tissue. A d ditio na l
ly, C20:4ra6 w as 7.6% in the digestiv e gland; it
wa s very hig h com paring to m an tle (RAKSHIT et
al., 1997). In edib le snail H. aspersa maxima,
C18:2ra6 was rather a lot, b etween 44 .79-51.19%
(MILINSK et al., 2006). In contrast, a comp a rison
between the com ponen ts acid s of th e cephalo-
pedal, digestive gland and w h ole bo d y o f H. lu-
corum show ed som e po ints o f interest; C18:3ra3
wa s at high p ercentages in the dige stive glan d ;
th e percen ta g e s o f C22:0 varied from 2.10% (in
the digestive glan d ) to 4.19% (in the wh ole body);
C12:0, C13:0, C14:0, C15:0, C20:0, C14:1ra7,
C17:1ra7 and C22:6ra3 w ere detected less than
1% in all tissues; C20:1ra9 is present in signif
ican t am oun t (4.47%) in the cep h alo pedal tis
sue (Table 1). S n ail ceph a lop edal is considere d
as a storage organ (JOHNS et al., 1979), prob a
bly, the cephalopedal stored this fatty acid for
fu r th e r meta bolic activities. C20:1ra9 was also
ob tained in h igh percentages in U. elongatulus
ce p haloped a l (EKİN and BASHAN, 2010).
The Xra6/Xra3 ra tio ha s been sugg e s ted to be
usefu l ind ica tor fo r com pa ring n utritio n al v al
ues of tissue s lipids. Th e ra tio of ra6/ra3 was
9.07 (in the gon a d), 7.26 (in the mantle), 6.02 (in
th e cephalopeda l), 4.86 (in the wh o le b o d y) a n d
4.0 6 (in the dig e s tive g lan d ) (Table 1). T he p er
centage s of ra6 w as 5 0 .27, 45.4 2 , 41.04, 42.81
and 41 .54% in th e gonad , m a ntle, d igestiv e
glan d , ceph aloped al and whole body, resp ec
tive ly (Table 1). In addition, L. maximus, P. an-
dersoni, A. ater slu gs and H. sp. H. sportella., V.
columbiana (ZHU et al., 1994) species contain e d
hig h a m oun t o f Xra6 than Xra3. H owever, in the
m ost of the previou s studie s, it was rep o r ted
th at the pe rc e n tage o f Xra6 w as low er than Xra3
in marine mo lluscs (ABAD et al., 1995; PAZOS
et al., 2003). Fish is we ll kn o wn to b e th e m ajor
so urce of ra3 fa tty acids in the d iet and p e o p le
have b e e n aware of the h ealth ben efits asso c i
ated w ith co n su min g fish. The usefu l o>3 in fish
flesh are C20:5ra3 a n d C22:6ra3 (ÖZ OG u l et al.,
20 0 5 ). Unlike fish and m arine gastropods, lev
el o f ra3 in H. lucorum accou n ted for low qu an
tity. C22:6ra3 level va rie d fro m 0.03% (in the
gonad) to 0.22% (in the w hole body) and level
58 Ital. J. Food Sci., vol. 26 - 2014
Table 1 - Fatty acid profiles of selected tissues from edible snail Helix lucorum.
Fatty
acids Gonad
(Mean^±S.D.)« Mantle
(Mean^±S.D.)^ Digestive gland
(Mean^±S.D.)^ Cephalopedal
(Mean^±S.D.)« Whole body
(Mean^±S.D.)«
Saturated
C12:0 0.07±0.01a 0.03±0.01 b 0.04±0.01b -0.09±0.02a
C13:0 -0.02±0.01 a 0.03±0.01a 0.06±0.01 b 0.07±0.01 b
C14:0 0.30±0.03a 0.66±0.05b 0.89±0.08c 0.40±0.05a 0.52±0.04d
C15:0 0.19±0.02a 0.31 ±0.03b 0.36±0.04b 0.25±0.03a 0.72±0.06c
C16:0 10.94±0.86a 14.04±1.19b 13.17±1.13b 8.95±0.81 c 12.55±1.07ab
C17:0 1.44±0.13a 1.25±0.11a 2.13±0.19b 2.19±0.20b 0.70±0.07c
C18:0 10.78±0.88a 11.65±1.01a 8.39±0.78b 11.42±1.12a 8.92±0.75b
C20:0 0.14±0.02a 0.24±0.03b 0.22±0.03b 0.19±0.02b 0.16±0.02a
C22:0 3.01±0.18a 3.05±0.22a 2.10±0.16b 3.45±0.25a 4.19±0.32c
ESFA 26.87±1.33a 31.25±1.65b 27.33±1.43a 26.91±1.27a 27.92±1.39a
Monoenoic
C14:1m7 0.04±0.01a 0.10±0.02b 0.06±0.01a -0.11±0.02b
C16:1m7 3.82±0.33a 3.72±0.29a 3.53±0.26a 3.22±0.24a 2.98±0.23a
C17:1m7 0.21±0.03a 0.08±0.01b 0.06±0.01b 0.11±0.02c 0.12±0.02c
C18:1m9 13.14±1.01a 11.23±0.92b 17.18±1.18c 15.76±1.12ac 18.20±1.27c
C20:1m9 0.27±0.03a 1.79±0.15b 0.29±0.04a 4.47±0.34c 0.52±0.05d
EM UFA 17.48±1.15a 16.92±1.13a 21.12±1.20b 23.56±1.26c 21.93±1.18b
Polyenoic
C18:2m6 16.12±1.17a 18.77±1.35b 24.44±1.56c 19.21±1.43bc 20.78±1.48bc
C18:3m3 2.83±0.22a 4.34±0.37b 7.30±0.54c 4.99±0.31b 6.41±0.53bc
C20:2m6 10.52±1.04a 10.09±1.17a 4.78±0.31b 8.28±1.14c 6.55±0.62d
C20:3m6 4.25±0.37a 3.09±0.22b 1.76±0.15c 1.86±0.16c 2.09±0.17c
C20:4m6 1749±1.26a 12.25±1.05b 8.89±0.77c 12.76±1.12b 11.23±1.02b
C20:5m3 2.68±0.24a 1.88±0.16b 2.70±0.21a 2.03±0.19b 1.91±0.13b
C22:5m6 1.89±0.19a 1.22±0.09a 1.17±0.16a 0.70±0.08b 0.89±0.10b
C22:6m3 0.03±0.01 a 0.04±0.01a 0.10±0.02b 0.09±0.02b 0.22±0.03c
m6 50.27 45.42 41.04 42.81 41.54
m3 5.54 6.26 10.10 7.11 8.54
m6 / m3 9.07 7.26 4.06 6.02 4.86
EPUFA 55.81±2.12a 51.68±2.03b 51.14±2.03b 49.92±1.99b 50.08±2.08b
Results expressed as percentage of total fatty acids methyl esters.
*Values are means ± S.D (Standard Deviation) for three samples of triplicate analysis.
**Means followed by different letters in the same line are significantly different (P < 0.05) by Tukey's test.
ESFA: Saturated Fatty Acids, EMUFA: Monounsaturated Fatty Acids, EPUFA: Polyunsaturated Fatty Acids, ra6: Total of omega 6 fatty acids, ra3: Total of ome-
ga 3 fatty acids.
Table 2 - Major fatty acids compositions (%) of the tissues from Helix lucorum.
Tissues Predominant six fatty acids of Helix lucorum and their percentages (%) Total percentages (%)
Gonad C20:4m6 C18:2m6 C18:1m9 C16:0 C18:0 C20:2m6 78.99
(17.49) (16.12) (13.14) (10.94) (10.78) (10.52)
Mantle C18:2m6 C16:0 C20:4m6 C18:0 C18:1m9 C20:2m6 78.03
(18.77) (14.04) (12.25) (11.65) (11.23) (10.09)
Digestive gland C18:2m6 C18:1m9 C16:0 C20:4m6 C18:0 C18:3m3 79.37
(24.44) (1718) (13.17) (8.89) (8.39) (7.30)
Cephalopedal C18:2m6 C18:1m9 C20:4m6 C18:0 C16:0 C20:2m6 68.10
(19.21 ) (15.76) (12.76) (11.42) (8.95) (8.28)
Whole body C18:2m6 C18:1m9 C16:0 C20:4m6 C18:0 C20:2m6 78.23
(20.78) (18.20) (12.55) (11.23) (8.92) (6.55)
of C20:5ra3 wa s b etwe e n 1.88% (in th e m an tle)
and 2.7 0 % (in the d igestive gland) (Table 1). The
highes t va lue o f ra3 w as foun d to be 10.10% in
th e digestiv e gla n d because o f relativ ely high
percentage o f C18:3ra3 (7.30%) (Table 1). The
differen ces in th e level o f ra3 and ra6 fatty acids
of species is p oten tia lly d u e to d ieta ry factors
becau se marin e plank ton are rich in ra3 fatty
acids, wh ile terrestrial an d fresh w ater p lan k
to n s are rich in ra6 a c ids (SARGENT, 1976). A d
ditionally, end o geno u s factors such as ge ne t
ic, p hysiology, b iochem ical rea c tion etc. m ay
Ital. J. Food Sci., vol. 26 - 2014 59
Table 3 - Total lipid content of the tissues from Helix lucorum (g/100 g wet tissue ±S.D. % on basis o f total lipid).
Tissues Gonad Mantle Digestive gland Cephalopedal Whole body
Total lipid 2.52±0.40 0.93±0.14 3.54±0.37 1.21 ±0.13 1.09±0.23
affe ct accu mulatio n of ra3 and ra6 fatty acids
in the sp e c ies tissu e s.
The maxim um am o u nt o f ESFA (saturated fat
ty acids), E M UFA (m o n ounsaturated fa tty acids)
and EPUFA (polyu n satu rated fatty acids) were
fou n d in the mantle (31.2 5% ), in the cep h alo
pedal (23.56%) and in the gona d (55.81%), re
sp ectively. It is o f the interest th at a considera
ble a m ount o f EPUFA wa s detected in all tissue
analyses. EPUFA level o f each tissue w as h igh er
th an 50% (ex cept cephalopedal tissue w h ich is
49.92% ) nea rly equal to su m of ESFA an d EM UFA
levels. E P U FA levels o f the tissues d ete c ted high
bec au se o f h igh con ce ntra tion of C18:2ra6,
C20:2ra6 and C20:4ra6 (Table 1). It w as repo rt
ed that EPUFA level wa s higher than EM UFA and
ESFA levels in L. maximus, P. andersoni and A.
ater slugs (ZH U et al., 1994). In edible snail H.
aspersa, sum o f EM U FA and EP U FA w as 55.02 %
and EP U FA wa s at the highest level (ÇAGILTAY et
al., 2011). In an another ed ible snail H. aspersa
maxima, EPUFA levels were also obtained at high
percen tages (b etw een 46.40-54.97%) (MILINSK
et al., 2006). On the oth er hand, it h as been ex
pre ssed that high ESFA (37.87 % ) and low EPUFA
(25.83% ) level w ere foun d in edible snail H. po
matia (ÖZO G ul et al., 2005). Briefly, tissues of
H. lucorum are ch aracterized by high p e r c e n tag
es of PUFA. However, lipid and fatty acid con
ten t of a sn a il tissue m ostly depends o n sev e r
al fa ctors such as seasona l changes, nu trition
al availability, environm e n tal factor, physiology,
rep rodu c tion, tissue functions, etc. T he notable
diffe rence being the high level of EPUFA w ith a
so m ewhat decreased relativ e c o n centration level
of ES FA and EM UFA in th e snail tissues prob a
bly rela tive to tem peratu re conditions because,
th e sam p les we re collected during A pril w he n
tem pera ture is still lo w (approxim ately 15°C).
Prosta g land in s are c o ns iderab ly im portan t
molecules in m ollusc physio logy such as possi
ble ren al function, ion regulation in gill, and re
productive functions in gonad (STANLEY-SAMUEL-
SON, 1987). It is em path ized that egg production
in freshw ater snail H elisoma durgi w a s stimu lat
ed by prostaglan din s (KUNIGELIS an d SALEUD-
DIN, 1986). In com parison with other fatty ac
ids, C20:4ra6 (precursors of prostaglandins) w as
in fair am ount in the tissues partic u larly in the
gon ad (17.49%). Prob ably, this high valu e is re
lated to rep rod u ction activity or accelerated fe e d
ing activities after em erging from hibern a tion.
The digestive gland (3.54%) and gonad (2.52%)
of the sn a il exh ibited m axim u m reserve o f total
lipid wh ereas m an tle (0.93%) and cephalopedal
(1.21% ) contain ed rela tively low quantities (Ta
ble 3). Th is signifies that dig e stive gland a n d go
nad are m ore a ctive organ s. It was declared that
th e se organs h ad m ajo r proportion o f total lipid
in gastropod (VOOGT, 1983). In the study of T.
telescopium, to tal lip id am oun t w as foun d to be
36 .91 % in the digestive glan d , 13.44% in the
mantle, 11.67% in the ce p halopedal (RAKSHIT et
al., 1997). Th e re su lts are ve ry high fo r an edible
lan d snail. Th e most of the stu d ies m entioned
th at land snails contain low quantities o f lipid
(ÖZOG ul et al., 2005; MURPHY, 2001). Total li
pid percentages o f H. aspersa maxima varied be
tw een 0 .45% and 2.66% (MILINSK et al., 2006).
In conclu sion, given im proved cu ltural tech
niques, H. lucorum b e c o m e the po tentia l a rich
source of un sa tu ra te d fatty acids; C18:1ra9,
C18:2ra6, C20:2ra6 a n d C20:4ra6 (ra6 fa tty acids)
th at the snail m eet contain s s ignificant am ount
of essentia l fatty acid (C18:2ra6). P UF A s with
more than 20 C atom s are ind icatin g that the
use of this food is good for diets, irrespective of
to tal lipid content. In a d dition, the resu lts can
be im p orta n t guid e for fu rth er inv estigation on
physiolog ical, b ioch em ical and system atic stud
ies o f mollu scs.
ACKNOWLEDGEMENTS
The author is grateful to Mehmet Başhan, dvan Seşen and
Elif Cengiz Satar for their statistical, systematic and exper
imental support.
REFERENCES
Abad M., Ruiz C., Martinez D., Mosquera G. and Sanchez
J.L. 1995. Seasonal variation of lipid classes and fatty ac
ids in flat oyster, Ostrea edulis, from San Cibrian (Gali
cia, Spain). Comp. Biochem. Physiol. 110C (2): 109-118.
Bligh E.G. and Dyer W.J.A. 1959. A rapid method of total
lipid extraction and purification. Can. J. Biochem. Physi
ol. 37: 911-917.
Caers M., Coutteau P., Cure K., Morales V., Gajardo G.
and Sorgeloos P. 1999. The Chilean scallop Argopecten
purpuratus (Lamarck, 1819): I. fatty acid composition
and lipid content of six organs. Comp. Biochem. Physi
ol. 123B: 89-96.
Çagıltay F., Erkan N., Tosun D. and Selçuk A. 2011. Ami
no acid, fatty acid, vitamin and mineral contents of ed
ible garden snail (Helix aspersa). J. FisheriesSciences.
com. 5(4): 354-363.
Ekin I. and Basjhan M. 2010. Fatty acid composition of se
lected tissues of Unio elongatulus (Bourguignat, 1860)
(Mollusca: Bivalvia) collected from Tigris River, Turkey.
Turk. J. Fish. Aquat. Sci.10: 445-451.
Ekin I., Bashan M. and Sesen R. 2011. Possible seasonal
variation of the fatty acid composition from Melanopsis
60 Ital. J. Food Sci., vol. 26 - 2014
praemorsa (L., 1758) (Gastropoda: Prosobranchia), from
southeast Anatolia, Turkey. Turk. J. Biol. 35:203-213.
Folch J., Lees M. and Sloane-Stanley G.H. 1957. A simple
method for the isolation and purification of total lipids
from animal tissues. J. Biol. Chem. 226: 497-509.
Go J.V., Rezanka T., Srebnik M. and Dembitsky V.M. 2002.
Variability of fatty acid component of marine and fresh
water gastropod species from the littoral zone of the Red
Sea, Mediterranean Sea and Sea of Galilee. Biochem.
Syst. Ecol. 30: 819-35.
Jess S. and Marks R.J. 1995. Population density effects on
growth in culture of the edible snail Helix aspersa var.
maxima. J. Mollusc. Stud. 61: 313-323.
Johns R.B., Nichols P.D. and Perry G.J. 1979. Fatty acid
components of nine species of molluscs of the littoral
zone from Australian waters. Comp. Biochem. Physiol.
65 B: 207-214.
Kunigelis S.C. and Saleuddin A.S.M. 1986. Reproduction
in the freshwater gastropod Helisoma: involvement of
prostaglandin in egg production. Int. J. Inver. Rep. Dev.
10: 159-167.
Miletic I., Miric M., Lalic Z. and Sobajic S.1991. Composi
tion of lipids and proteins of several species of molluscs,
marine and terrestrial, from the Adriatic Sea and Serbia.
Food Chem. 41: 303-308.
Milinsk M.C., Padre R., Hayashi C., De Oliveira C.C., Visen-
tainer J.V., De Souza N.E. and Matsushita M. 2006. Ef
fect of food protein and lipid contents on fatty acid pro
file of snail (Helix aspersa maxima) meat. J. Food Com
pos. Anal. 19: 212-216.
Misra K.K., Shkrob I., Rakshit S. and Dembitsky V.M. 2002.
Variability in fatty acids and fatty aldehydes in different
organs of two prosobranch gastropod mollusks. Biochem.
Syst. Ecol. 30: 749-761.
Murphy B. 2001. Breeding and growing snails commercial
ly in Australia RIRDC-Rural Industries Research Devel
opment Corporation, Kingston.
Özogul Y., Özogul F. and Olgunoglu I.A. 2005. Fatty acid
profile and mineral content of the wild snail (Helix poma-
tia) from the region of south of the Turkey. Eur. Food Res.
Tech. 221: 547-549.
Pazos J.A., Sanchez L.J., Roman G., Perez-Parelle M.L. and
Abad M. 2003. Seasonal changes in lipid classes and fat
ty acids composition in hepatopancreas of Pecten maxi
mus. Comp. Biochem. Physiol. 134B: 367-380.
Rakshit S., Bhattacharyya D.K. and Misra K.K. 1997. Dis
tribution of major lipids and fatty acids an estuarine gas
tropod mollusc Telescopium telescopium. Folia Biologica
(Krakow). 45: 83-87.
Sargent J.R. 1976. The structure, metabolism and func
tion of lipids in marine organisms. In: Biochemical
and Biophysical Perspectives in Marine Biology", D.C.
Malin and J.R. Sargent (Ed.), pp.149-212, Academic
Press, London.
Stanley-Samuelson D.W. and Dadd R.H. 1983. Long chain
polyunsaturated fatty acids: Patterns of occurrence in in
sects. Biochemistry. 13: 549-558.
Stanley-Samuelson D.W. 1987. Physiological roles of pros
taglandins and other eicosanoids in invertebrates. Biol.
Bulletin. 173: 92-109.
Stavrakakis H.J., Mastronicolis S.K. and Kapoulas V.M.
1989. Lipid composition and structural studies on lip
ids from the land snail Eobania vermiculata. Z. Natur-
forsch. 44C: 597-608.
Wenne R. and Polak L. 1989. Lipid composition and stor
age in the tissues of the Macoma balthica. Biochem. Syst.
Ecol. 17: 583-587.
Voogt P.A. 1983. Lipids: their distribution and metabolism.
In: The mollusca", K.M. Wilbur (Ed.). pp. 329-370, Aca
demic press. New York, London.
Yıldırım M.Z. and Kebapçı Ü. 2004. Slugs (Gasteropoda: Pul-
monata) of the Lakes Region (Göller Bölgesi) in Turkey.
T.J. Zoology. 28: 155-160.
Zhu N., Dai X., Lin D.S. and Cornor W.E. 1994. The lipids
of slugs and snails: Evolution, diet and biosynthesis. Lip
ids. 29: 869-875.
Paper received April 30, 2013 Accepted August 2, 2013
Ital. J. Food Sci., vol. 26 - 2014 61
... the fatty acid distribution of a large number of commercially important marine and freshwater molluscs have been reported and reviewed in varying degrees of details (AcKMAN, 2000;KArAKOLtsID-Is et al., 1995). Lipids from marine, freshwater and edible land molluscs are more extensively studied (ÖZOĞUL et al., 2005;MILINsK et al., 2006;MILEtIc et al., 1991;rAKsHIt et al., 1997;EKİN and bAŞHAN, 2010;EKİN et al., 2012EKİN et al., , 2014 than those from nonedible terrestrial members. Nevertheless, nonedible land snails deserve special attention from the point of their evolutional relationship, roles in food chain, nutritional value, taxonomic and possible benefits in cosmetic, medicine and biochemistry. ...
... Furthermore, only few studies are present on fatty acid distribution of mollusc organs and tissues. Macoma balthica (WENNE and POLAK, 1989), Telescopium telescopium (rAKsHIt et al., 1997), Argopecten purpuratus (cAErs et al., 1999), Bellamya bengalensis, Pila globosa (MIsrA et al., 2002), Unio elongatulus (EKİN and bAŞHAN, 2010), Corbicula fluminalis (EKİN, 2012), H. lucorum (EKİN 2014) are some of known mollusc species, tissue and organs studied. ...
... 79%-51.19% (MILINsK et al., 2006) and this fatty acid was also found good amount in edible snail H. lucorum (EKİN, 2014). Most likely, these different data stem from the requirement of the fatty acid for snail species. ...
Article
Full-text available
In the present work, main organs (digestive gland, cephalopedal, gonad and mantle) and lipid classes (total, neutral and phospholipid) of land snails Assyriella escheriana and Assyriella gutta-ta from southeastern Anatolia were examined for their fatty acids. the major components detected in both of the species were c16:0, c18:0, c18:1ω9, c18:2ω6, c18:3ω3, c20:2ω6 and c20:4ω6. c18:2ω6 was identified as the primary fatty acid ranging from17.07% to 28.12% in A. guttata and 18.02% to 27.43% in A. escheriana. the proportions of c20:4ω6 modified to form prostaglandins that are directly involved in regulation of reproduction, ranged from10.01% to 20.30% in A. es-cheriana and 11.05 % to 16.58% in A. guttata. taking into consideration that ΣPUFA levels were always higher than ΣsFA and ΣMUFA levels in all treatments of both species. this was an expected finding for the snails collected during the breeding season because PUFA plays an important role as precursors for signal-transduction involved in the regulation of mating and reproduction. A significant amount of c20:2ω6 was concentrated in the cephalopedal of A. guttata (13.42%) and A. escheriana (14.93%). Probably, cephalopedal serves as a storage organ of this component. consequently , the findings revealed that the snail's fatty acid profiles were qualitatively similar, but quantitatively there were some differences. Most important of all, tissues of the snails were good source of essential fatty acids (c18:2ω6 and c18:3ω3) and PUFA, particularly omega 6 fatty acids.
... Fatty acid compositional data for widely consuming organisms such as fish, squid, octopus, crustacean, livestock and poultry are available in the literature; however, fatty acids content of phospholipid subclasses in edible land snails is meager. Most of the studies about fatty acid of terrestrial and aquatic mollusc of Turkey are published by us [7][8][9]. In the current study, the fatty acid composition of two tissues from H. lucorum was analyzed to assess the nutritive value of its meat and thereby to create awareness about fatty acid distribution of phospholipid subclasses including PE, PC, PI and PS. ...
... In the total body, the highest value was 9.96 and 12.95 in PI and PS, respectively. In our previous studies on terrestrial and freshwater molluscs, ω6 PUFA levels were found higher than ω3 PUFA [7][8][9]. In agreement with our findings, Σω6/Σω3 ratio was also defined to be high in A. ater, L. maximus, P. andersoni, slugs and H. sp., H. sportella, V. columbiana snails [22]. ...
Article
Yenilebilir salyangoz Helix lucorum'un sefalopedal ve total vücut dokusundan elde edilen fosfolipit alt sınıflarına ait yağ asitlerinin belirlenmesi] ABSTRACT Objective: The objective of the study was to examine the nutritive value of Helix lucorum meat and to create awareness about fatty acid composition of phospholipid subclasses of the total body and cephalopedal tissues of the snail. Methods: Thin layer chromatography plates contained lipid samples placed in the chromatography tank containing: chloroform/ethanol/water/triethylamine. The phospholipid subclasses were dissolved in about 5 ml of methanol and 5 drop of sulfuric acid. The mixture was refluxed for 2 h to form fatty acid methyl esters at 85 °C. Fatty acids were detected by Gas chromatography. Results: The most noteworthy result was the high level of C20:2ω6 in PE (10.49%-11.35%) and PC (17.33%-12.96%). Appreciable quantity of essential fatty acid C18:2ω6 was determined in PC (20.85%-17.46%) and PE (16.88%-17.53%) from both tissues. Precursor of eicosanoids, C20:4ω6 was found apparently high in PI, PS and PE of the total body. The highest level of ΣPUFA was 63.90% in PE from total body whereas the highest level of ΣSFA was 60.79% in PI from the cephalopedal. ΣMUFA level was pretty low in PI, PS and PE. Conclusion: The study is a guide for biochemical and nutritional value of edible snails and can be useful for further investigation on physiological and systematic studies of other species. ÖZET Amaç: Bu çalışmanın amacı, Helix lucorum'un besin değerini incelemek ve salyangozun total vücut ve sefalopedal dokularına ait fosfolipid alt sınıflarının yağ asidi kompozisyonu ile ilgili farkındalık yaratmaktır. Metod: Lipit örnekleri içeren ince tabaka kromatografi plakaları, kloroform/etanol/su/trietila-min içeren kromatografi tankına yerleştirildi. Elde edilen fosfolipid altsınıfları, yaklaşık 5 ml metanol ve 5 damla sülfürik asit içinde çözünür hale getirildi. Karışım, yağ asidi metil esterle-rini oluşturmak için 2 saat boyunca 85 °C de karıştırılıp ısıtıldı. Yağ asitleri Gaz kromatografi cihazı ile tespit edildi. Bulgular: C20:2ω6 nin, PE (%10.49-%11.35) ve PC (%12.96-%17.33) deki yüksek oranı en dikkat çekici sonuçtu. Her iki dokunun PC (%20.85-%17.46) ve PE (%16.88-%17.53) sin-de, esansiyel yağ asidi olan C18:2ω6 nın oranı yüksekti. Eikosanoidlerin öncü bileşeni olan C20:4ω6, total vücut dokusuna ait PI, PS ve PE (%28.37, %30.91 ve %26.48) de yüksek bulun-du. ΣPUFA en yüksek oranı %63.90 ile total vücut PE sinde, ΣSFA en yüksek oranı ise %60.79 ile sefalopedal PI sinde tespit edildi. ΣMUFA oranı ise PI, PS ve PE de oldukça düşüktü. Sonuç: Bu çalışma, yenilebilir salyangozların besinsel ve biyokimyasal değeri için rehber ni-teliğindedir ve diğer türler ile ilgili ilerde yapılacak sistematik ve fizyolojik araştırmalar için yararlı olacağına inanılmaktadır. Anahtar Kelimeler: Fosfolipid altsınıfları, yağ asitleri, Helix lucorum, yenilebilir kara sal-yangozu Çıkar Çatışması: Yazarların çıkar çatışması yoktur. obtained herein adds to our knowledge of the comparative biochemistry of the fatty acid composition of representative edible gastropods. Material and Methods Sample collection and lipid extraction Snail samples were collected from the Hevsel Gardens, in Diyarbakır (Altitude: 583 m, Coordinate: N 37° 55.2'/E 40° 13.8'), Turkey and transported to laboratory for sample preparation within 1 h of collection. The samples were received in the month of May, 2013. Individually, eighteen snails (nine for cephalopedal, nine for total body) similar size (length: 4±1.20 cm, wet flesh weight: 12±0.50 g) were sampled for each tissue lipid analysis. Samples were washed with distilled water and their shells were removed. Then, the total body and cephalopedal parts were dissected out and immediately used for analyses. Total lipids were extracted with 10 ml of chloroform-methanol (2:1). During the extraction process, autoxidation of unsaturated fatty acids was minimized by adding 50 ml of 2% butyl-ated hydroxytoluene (BHT) in chloroform to each sample. Nonlipid contaminants were removed by extraction with 5 ml of 0.88% aqueous KCl [10]. The lipid containing lower phase was separated and evaporated under a stream of nitrogen at room temperature just to dryness. Separation of phospholipid subclasses by one-dimensional TLC Thin layer chromatography plates (TLC) were air-dried in a fume hood and placed in the preservation tank until used. They were thoroughly wetted with boric acid solution in ethanol (2.3% w/v), drained 5 min in a fume hood and dried for 15 min at 100°C in an oven prior to using. Lipid samples were quickly deposited on the plates as 1 or 2 cm parallel streaks in the concentration zone and placed in the chromatography tank containing: chloroform/etha-nol/water/triethylamine (30/35/7/35, v/v). The migration time was about 2 hours. Then, plates were dried in a fume hood and sprayed with 0.2%, 2'7 dichlorofluorescein in ethanol. After viewing under UV light, spots belonging to phospholipid subclasses were scraped into methylation container [11]. Preparation of fatty acid methyl ester and GC conditions The lipid sample was dissolved in about 5 ml of methanol, and 5 drop of sulfuric acid was added. The mixture was refluxed for 2 h to form fatty acid methyl esters (FAME) at 85°C. Then, FAME was extracted from the mixture with n-hexane and concentrated on a Rota evaporator at 40°C to reduce their volume to 1 ml for analysis. The content of FAME was analyzed by capillary gas chromatography using a Shimadzu GC-2010 Plus equipped with a flame ion-ization detector (FID) and a fused silica capillary column (DB-23) (Bonded 50% cyanopropil, 30 m×0.25 mm×0.25 mikrom film thickness, J&W Scientific, Folsom, CA, USA).The flow rates of compressed air and hydrogen were 300 ml/min, 30ml/min, respectively. Helium was used as Turk J Biochem 2015; 40(2):132-139 133 Ekin et al.
... Fatty acid compositional data for widely consuming organisms such as fish, squid, octopus, crustacean, livestock and poultry are available in the literature; however, fatty acids content of phospholipid subclasses in edible land snails is meager. Most of the studies about fatty acid of terrestrial and aquatic mollusc of Turkey are published by us [7][8][9]. In the current study, the fatty acid composition of two tissues from H. lucorum was analyzed to assess the nutritive value of its meat and thereby to create awareness about fatty acid distribution of phospholipid subclasses including PE, PC, PI and PS. ...
... In the total body, the highest value was 9.96 and 12.95 in PI and PS, respectively. In our previous studies on terrestrial and freshwater molluscs, ω6 PUFA levels were found higher than ω3 PUFA [7][8][9]. In agreement with our findings, Σω6/Σω3 ratio was also defined to be high in A. ater, L. maximus, P. andersoni, slugs and H. sp., H. sportella, V. columbiana snails [22]. ...
Article
Full-text available
Objective: The objective of the study was to examine the nutritive value of Helix lucorum meat and to create awareness about fatty acid composition of phospholipid subclasses of the total body and cephalopedal tissues of the snail. Methods: Thin layer chromatography plates contained lipid samples placed in the chromatography tank containing: chloroform/ethanol/water/triethylamine. The phospholipid subclasses were dissolved in about 5 ml of methanol and 5 drop of sulfuric acid. The mixture was refluxed for 2 h to form fatty acid methyl esters at 85 °C. Fatty acids were detected by Gas chromatography. Results: The most noteworthy result was the high level of C20:2ω6 in PE (10.49%-11.35%) and PC (17.33%-12.96%). Appreciable quantity of essential fatty acid C18:2ω6 was determined in PC (20.85%-17.46%) and PE (16.88%-17.53%) from both tissues. Precursor of eicosanoids, C20:4ω6 was found apparently high in PI, PS and PE of the total body. The highest level of ΣPUFA was 63.90% in PE from total body whereas the highest level of ΣSFA was 60.79% in PI from the cephalopedal. ΣMUFA level was pretty low in PI, PS and PE. Conclusion: The study is a guide for biochemical and nutritional value of edible snails and can be useful for further investigation on physiological and systematic studies of other species.
... The fatty acid compositions of selected tissues of H. lucorum including gonad, mantle, digestive gland, cephalopedal and whole body of H. lucorum were studied in detail in our previous studies [25]; however, the fatty acid composition of lipid classes of E. vermiculata and L. flavus were not studied. As a result, current study can be a significant guide for nutritional value and quantitative analysis of edible snails of Türkiye. ...
Article
Full-text available
The purpose of this work is to reveal the fatty acid composition of phospholipids, neutral and total lipid content of edible land snails Helix lucorum, Eobania vermiculata and non-edible land slug Limax flavus (Gastropoda: Pulmonata). The analyses revealed that the snails and slug are rich in C16:0, C18:0, C18:1ω9 and C18:2ω6 acids. Phospholipid fractions contained very high amounts of C20:4ω6 (15.37% in H. lucorum, 12.37% in E. vermiculata and 8.59% in L. flavus) which is the most important precursor of eicosanoids. The level of ΣPUFA, in edible snails, was found to be higher than ΣSFA and ΣMUFA. However, in the slug, ΣMUFA level was higher than ΣSFA and ΣPUFA levels in neutral and total lipid contents. Ʃω6 / Ʃω3 (Omega 6 / Omega 3) ratio was defined to be very high in the phospholipid of H. lucorum, E. vermiculata and L. flavus; 6.07, 8.29 and 5.39, respectively. Furthermore, the study showed that all three species are valuable sources of omega 6 and essential fatty acids; C18:2ω6 and C18:3ω6.
... The CAM and CAA fat, however, had significantly higher content of MUFA and PUFA acids. Although the literature appears scarce as to data on fatty acid content in edible snail fat (5,7,14,15,18,25,28), the available data serve to confirm the relationship between the SFA, MUFA, and PUFA proportions established in the present studies. The current literature data demonstrate that PUFA acids in CAM and CAA fat can account for from 34.38% up to as high as 57.06% of fatty acid content, MUFA may represent from 20.06% to 23.82%, whereas SFA make up from 22.2% to 28.76% (5,15,16). ...
Article
Full-text available
Introduction: The objective was to determine the content of fatty acids in edible snail fat by snail species, collection site, and processing stage. Material and Methods: The research material comprised 180 edible fat samples from the three genera of edible snails collected in Poland: free-living Helix pomatia (HP) and two cultivated Cornu subspecies: C. aspersa maxima (CAM) and C. aspersum aspersum (CAA). All snails came from the Greater Poland and Lower Silesian Provinces: HP from their natural habitat and CAM and CAA from heliciculture farms. The studies focused on the raw meat, cooked meat, and frozen meat processing stages. Fatty acid (FA) profiles were determined by the gas chromatography method. Results:Helix pomatia fat showed a higher saturated fatty acid (SFA) content, whereas the fat of Cornu genus snails had a higher unsaturated fatty acid (UFA) component, i.e. monounsaturated fatty acid (MUFA) and polyunsaturated fatty acid (PUFA). Thermal processing of snail meat increased all the determined SFA and decreased all the PUFA values, and increased the content of C18:1, C20:1, and C22:1 acids in the MUFA group. The material collection site had limited impact on FA content as differences were noted only in levels of C18:1, C18:2 n6, and C20:5. The differences pertained only to the fat of farmed snails of the Cornu genus. Conclusion: Due to the high content of UFA and a favourable ratio of n6:n3 acids and PUFA:SFA, snail fat can be regarded as nutritionally valuable.
... In several recently published laboratory research studies, the euthanasia of gastropods was accomplished through diverse methods including freezing, 44 live dissection, 16,31 and lidocaine gel for anesthesia before dissection. 34 Another study did not state exact processes used for euthanasia, because of a waiver of an animal ethic statement or formal approval for research on gastropods (that is, it was not required). ...
Article
Full-text available
The euthanasia of invertebrates used in scientific investigations poses unanswered questions regarding the rapid induction of unconsciousness with minimal distress and pain. Relative to vertebrates, invertebrates' sensory experience of pain, nociception, and physiologic response to aversive stimuli are poorly characterized. The scientific communities in the European Union, Canada, United States, Australia, and New Zealand join in consensus regarding the need to address alleviation of pain and distress in cephalopods (octopus, squid, and so forth), which have the best-characterized nervous system among invertebrates. In the current study, we evaluated various euthanasia techniques in a terrestrial gastropod species, with priority on animal wellbeing, scientific variability, feasibility in both field and laboratory settings, and acceptability by personnel. In addition, we demonstrated that the 2-step method of euthanasia described in the AVMA Guidelines as acceptable for aquatic invertebrates is effective for terrestrial snails and meets all welfare and scientific requirements. This 2-step method first induces anesthesia by immersion in 5% ethanol (laboratory-grade ethanol or beer) followed by immersion in a euthanizing and tissue-preserving solution of 70% to 95% ethanol or 10% neutral buffered formalin. Furthermore, alternative methods of euthanasia for terrestrial snails commonly used in field research, such as live immersion in concentrated ethanol or formalin, were shown to be unacceptable. Copyright 2016 by the American Association for Laboratory Animal Science.
Article
Full-text available
Three families (Limacidae, Agriolimacidae and Milacidae) and 7 species, (Limacus flavus, Deroceras reticulatum. Deroceras berytensis, Mesolimax brauni, Mesolimax escherichi, Milax cf. altenai and Tandonia budapestensis) were identified from Lakes Region (Isparta, Burdur, and Afyon provinces). These include 1 endemic genus with 2 species. In this study some new habitat information and morphological data of the species are given. Additionally, Deroceras reticulatum, D. berytensis and Milax cf. altenai are new records for the area.
Article
Full-text available
The total lipids of the commercial land snail Eobania vermiculata (Gastropoda, Pulm onata, Stylom m atophora) are found to constitute a small percentage (0.8% ) of the wet tissue, which is comparable to that reported for other gastropods. Polar lipid components comprise 61.4% of the total lipids. The individual lipid classes obtained by column chromatographic fractionation were purified by preparative TLC or by column chromatography and their structure was confirmed by a combination of chromatographic and analytical determinations before and after mild alkaline hydrolysis and/or (dry) acid methanolysis and by IR analysis. Neutral lipids represent 36.4% of total lipids, containing cholesterol, cholesterol esters and triglycerides as their major components (26.2% , 29.1% and 25.5% respectively). They contain also a significant amount (14%) of free glyceryl ethers, which are found in a mollusc for the first time. The overall composition of the polar lipids (mol/100 mol lipid-P) was found as follows: Cardiolipin, 2.9; phosphatidylethanolamine, 24.9 (of which 19.8% plasmalogen analog); phosphatidylcholine, 49.2 (of which 45.6% glycerylether analog); ceramide aminoethylphosphonate, 7.5 plus 0.01 (another three minor species); diglyceride-am noethylphosphonate, 6.3; Sphingoethanolamine 1.65 (for the first time found and structurally studied in a land gastropod); and phosphatidic acid 1.1. Unsaturated fatty acyl groups represent about 72.6 and 44.1 respectively in phosphatidylethanolamine and phosphatidylcholine. A significant amount (70.5% ) of unsaturated fatty acids is concentrated in neutral lipids. The C 16:0 alk-1-enyl chain was found to predominate (55.6% ) in the side chains of ethanolamine plasmalogen. Batyl alcohol was found as the main glycerylether bound to choline phosphate (97.5% ). Saturated fatty acyl groups with 16 carbon atoms were main components (54%) of the major ceramide aminoethylphosphonate species.
Article
Full-text available
Possible seasonal variations of the fatty acid composition (neutral lipid, phospholipid, and total lipid content) of the freshwater snail Melanopsis praemorsa were investigated over the course of a year. Snail body lipids were fractionated by thin layer chromatography. Fatty acid composition of total body lipid, phospholipid, and neutral lipid of whole snail and total lipid of their algal food were analyzed by capillary gas chromatography and gas chromatographymass spectrometry. The most abundant fatty acids were C16:0, C18:0, C16:1ω7, C18:1ω9, C18:2ω6, and C18:3ω3 acids in the lipid analyses of the snail and in its food. Odd-numbered fatty acids and C20 polyunsaturated fatty acid structures were confi rmed by gas chromatography-mass spectrometry. Some diff erences were found in the percentages of phospholipid and neutral, total, and algal lipid. It is proposed that possible seasonal variations in the snail lipids are related to temperature: a positive correlation between the level of ΣSFA (total saturated fatty acids) in total body lipid, phospholipid, and neutral lipid fractions of the snail and temperature was observed, whereas ΣMUFA (total monounsaturated fatty acids) levels were negatively related with temperature. On the other hand, there were fl uctuations in the concentrations of ΣPUFA (total polyunsaturated fatty acids) in all analyses. In algae, maximal ΣSFA, ΣMUFA, and ΣPUFA levels were registered in summer, spring, and winter, respectively. In addition, C18:2ω6 acid percentages in winter and autumn were signifi cantly high in the algae.
Article
Full-text available
The total lipid fatty acid content of some organs and whole specimen of freshwater mussel Unio elongatulus were investigated. The mussels were collected in July in 2007 from Tigris River, Turkey. Fatty acid content of selected tissues and whole mussel were analyzed by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). In the analyses, predominant fatty acids were C16:0, C16:1ω7, C18:1ω9, C20:1ω9, C20:4ω6 and C20:5ω3. Analyses of selected organs (mantle, gills, foot and whole body) presented different and characteristic fatty acids profiles. In the gills C16:1ω7 (30.2%), C16:0 (17.4%) acids; in the mantle C18:1ω9 (20.3%), C16:0 (25.4%) acids; in the foot C16:0 (20.8%), C16:1ω7 (15.9%), C18:1ω9 (15.4%) acids and in whole body C16:1ω7 (27.6%), C16:0 (23.6%) acids were the most abundant constituents. Also the percentages of C20:4ω6 and C20:5ω3 acids, precursors of eicosanoids, were apparently high in the gills and foot. It is presumed that the chief fatty acids present in a particular organ are related to specific functions of the organ. In all of the tissue analyses, ΣMUFA levels were higher than ΣPUFA and ΣSFA levels. © Published by Central Fisheries Research Institute (CFRI) Trabzon.
Article
Full-text available
The nutritive and market value of meat of edible garden snail from northern Turkey was deter-mined. Protein, fat, ash, water and carbohydrate value of edible garden snail were found 9.87, 0.58, 1.07, 82.50 and 5.99 % wet weight, respectively. The results of this study have showed that garden snails are good sources of amino acid, fatty acid, vitamins and minerals. The ly-sine, isoleucine and leucine content from essential amino acids were 721, 467.57 and 611.50 mg/100g, respectively. The major amino acids detected were aspartic acid (996.814 mg/100g), glutamic acid (1405.158 mg/100g), alanine (1063.877 mg/100g), serine (1039.248 mg/100g). Total saturated fatty acid, monounsaturated fatty acid and polyunsaturated fatty acid were de-termined 28, 76, 20.66 and 34.38 %. The vitamin A, vitamin E, vitamin B 1 , B 2 , B 3 and B 6 of vitamins were 5.462, 0.887, 0.154, 0.065, 3.226 and 0.288 mg/100g wet wt, respectively. Min-eral analysis of garden snails showed that they are rich in calcium and potassium (1357 and 1054 mg/kg) and low in iron (5.21 mg/kg).
Chapter
This chapter describes the lipid composition and lipid distribution in molluscs. It describes how molluscs achieve and maintain a characteristic composition of lipids, despite the different lipid composition of their diet. Fatty acids might occur in free form, but they are mostly present in esterified form. They are found in sterol esters, acylglycerols, and phospholipids. Most fatty acids possess straight chains, but considerable amounts of branched-chain fatty acids can be present. The monobranched fatty acids comprise the iso- and the anteiso fatty acids. The common multibranched or isoprenoid fatty acids are 4,8,12-trimethyltridecanoic acid, 2,6,10,14-tetramethylpentadecanoic acid, and 3,7,11,15-tetramethylhexadecanoic acid. Generally double bonds in unsaturated fatty acids are methylene interrupted. However, a number of dienoic fatty acids are known in which the double bonds are non-methylene interrupted. The fatty acid composition in organisms is influenced by several external conditions. Among these are temperature and diet. Therefore, fatty acid composition in storage organs varies with the diet and that in the membranes with the temperature.
Article
Lipid fractions and fatty acid composition of different organs, viz., digestive gland, mantle, and foot of the gastropod Telescopium telescopium inhabiting estuarine waters of West Bengal, India were studied. Thin layer chromatography and subsequent colorimetric analyses revealed the presence of phospholipid, cholesterol, and, to a lesser extent, triglycerides. Considerable variation in the three classes of lipids was observed in the organs studied so far. Gas liquid chromatography analyses showed the presence of saturated fatty acids (16: 0, 18:0, 14:0), monoenoics (18:1, 16:1, 20:1), and polyenoic fatty acids (22:5 w6, 20:5 w3, 18:2) in varying amounts in the three organs. This may be related with a specific function of the organ. Polyunsaturated fatty acids are present in fair amounts in T. telescopium. The occurrence of arachidonic acid (20:4) in this gastropod may be related to salinity, as was pointed out by other workers.
Article
Most published analyses of the fatty acid compositions of insect tissue do not record long-chain polyunsaturated fatty acids beyond C18:3. When this is set against recent discoveries of important nutritional and prostaglandinogenic roles for arachidonic and other long-chain polyunsaturates in several insects of diverse taxa, the issue of a possible general occurrence of such material in insects assumes compelling interest. We used gas chromatographic methods to investigate the presence of fatty acids of more than 18 carbon atoms in lipid extracts from whole-animal and specific tissue preparations, and in particular fractions of lipid extracts. Results indicate that such compounds generally occur as a low proportion of the total fatty acids in whole-animal extracts and in neutral acyl fractions. Larger numbers and higher proportions of long-chain fatty acids were detected in extracts of certain tissues and in the phospholipid fractions of whole animal extracts than were found in the unfractionated whole-animal extracts. These findings show that long-chain polyunsaturated fatty acids are a regular component of the tissues of the insects examined and, in the light of their known nutritional, prostaglandinogenic and presumed structural roles are of considerable biological significance.
Article
The introduction of nanogram quantities of prostaglandin E2 (PGE2) into the female genital opening of mated animals was found to increase both the number of egg masses produced and the number of eggs per mass. The intrahaemocoelic administration of a thousand-fold higher concentration of PGE2 was without effect, suggesting an indirect role of prostaglandin(s) in the regulation of egg production.Prostaglandin (PG) synthetase activity in both the bursa copulatrix and ovotestis varied with the reproductive status. High PG synthetase activity was present in virgin animals, and lower activity was found in mated animals.Prostaglandins produced by the bursa copulatrix are proposed here to be involved in the production of a matedness factor, which acts upon the brain to initiate or modulate egg production. PG produced by the ovotestis may be involved in ovulation. A model is proposed for the involvement of PG in the regulation of reproduction in Helisoma.